Elocine Elie
About Elocine Elie
Elocine Elie serves as the Associate Director of Clinical Data Management at Deciphera Pharmaceuticals, where he has worked since 2023. He possesses extensive experience in clinical data management, having previously held similar roles at Intellia Therapeutics and ECOG-ACRIN Cancer Research Group.
Current Role at Deciphera Pharmaceuticals
Elocine Elie currently serves as the Associate Director of Clinical Data Management at Deciphera Pharmaceuticals. She has held this position since 2023, contributing to the management and oversight of clinical data processes. Her role involves ensuring the integrity and accuracy of clinical data, as well as leading a team to facilitate effective data management practices.
Previous Experience at Deciphera Pharmaceuticals
Elocine Elie has a history of working at Deciphera Pharmaceuticals, where she held multiple roles. She initially served as Manager of Clinical Data Management from 2020 to 2021, then progressed to Senior Manager in 2021, before taking on her current position. During her time at Deciphera, she managed clinical data flow and queries among a team, demonstrating her project management capabilities.
Experience at Intellia Therapeutics, Inc.
Before her current role, Elocine Elie worked at Intellia Therapeutics, Inc. as Associate Director of Clinical Data Management from 2022 to 2023. In this position, she continued to apply her expertise in clinical data management, further enhancing her skills in overseeing clinical trials and data integrity.
Education and Expertise
Elocine Elie earned her Bachelor of Science degree in Biology with a minor in Cultural Anthropology from Northeastern University, completing her studies from 2002 to 2006. Her educational background provides a strong foundation for her extensive experience in clinical data management, particularly in evaluating disease response using established criteria such as RECIST and RANO.
Background in Clinical Data Management
Elocine Elie has over 15 years of experience in clinical data management, beginning her career as a Project Coordinator at ECOG-ACRIN Cancer Research Group from 2006 to 2018. She has developed a thorough understanding of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines, which are essential for conducting clinical trials. Her experience includes managing work instructions, standard operating procedures (SOPs), and ensuring quality control of clinical data.